D-Index & Metrics Best Publications

D-Index & Metrics D-index (Discipline H-index) only includes papers and citation values for an examined discipline in contrast to General H-index which accounts for publications across all disciplines.

Discipline name D-index D-index (Discipline H-index) only includes papers and citation values for an examined discipline in contrast to General H-index which accounts for publications across all disciplines. Citations Publications World Ranking National Ranking
Medicine D-index 90 Citations 29,955 290 World Ranking 7644 National Ranking 262

Overview

What is he best known for?

The fields of study he is best known for:

  • Gene
  • Internal medicine
  • Genetics

Jan H. Veldink focuses on Amyotrophic lateral sclerosis, Genetics, Genome-wide association study, Single-nucleotide polymorphism and Disease. The study incorporates disciplines such as SNP, Neuroscience and Mutation in addition to Amyotrophic lateral sclerosis. Allele, Gene, Expression quantitative trait loci, Gene expression profiling and Haplotype are the primary areas of interest in his Genetics study.

His Genome-wide association study research includes themes of Quantitative trait locus, Genetic architecture, Genetic association, Locus and Genetic variation. His study looks at the relationship between Single-nucleotide polymorphism and fields such as Phenotype, as well as how they intersect with chemical problems. His Disease study integrates concerns from other disciplines, such as Endocrinology and Subclinical infection.

His most cited work include:

  • Genome-wide association study identifies five new schizophrenia loci (1474 citations)
  • A reference panel of 64,976 haplotypes for genotype imputation (1312 citations)
  • Systematic identification of trans eQTLs as putative drivers of known disease associations (1249 citations)

What are the main themes of his work throughout his whole career to date?

The scientist’s investigation covers issues in Amyotrophic lateral sclerosis, Genetics, Genome-wide association study, Internal medicine and Disease. Pathology covers Jan H. Veldink research in Amyotrophic lateral sclerosis. His Pathology research incorporates elements of Neuroscience and Spinal cord.

Single-nucleotide polymorphism, Gene, Locus, Allele and Genetic variation are among the areas of Genetics where the researcher is concentrating his efforts. Jan H. Veldink works mostly in the field of Genome-wide association study, limiting it down to topics relating to Genetic association and, in certain cases, Genetic architecture, as a part of the same area of interest. His Internal medicine research incorporates themes from Gastroenterology, Endocrinology, Surgery and Oncology.

He most often published in these fields:

  • Amyotrophic lateral sclerosis (58.05%)
  • Genetics (36.24%)
  • Genome-wide association study (22.82%)

What were the highlights of his more recent work (between 2017-2021)?

  • Amyotrophic lateral sclerosis (58.05%)
  • Genetics (36.24%)
  • Genome-wide association study (22.82%)

In recent papers he was focusing on the following fields of study:

Amyotrophic lateral sclerosis, Genetics, Genome-wide association study, Gene and Computational biology are his primary areas of study. Jan H. Veldink has included themes like C9orf72, Case-control study and Genetic association in his Amyotrophic lateral sclerosis study. Genome-wide association study is a subfield of Single-nucleotide polymorphism that Jan H. Veldink tackles.

His study focuses on the intersection of Single-nucleotide polymorphism and fields such as Frontotemporal dementia with connections in the field of Neuropsychology and Audiology. His studies deal with areas such as Genome, Short read, Sequencing data, Microsatellite and Locus as well as Computational biology. The Internal medicine study combines topics in areas such as Gastroenterology and Oncology.

Between 2017 and 2021, his most popular works were:

  • Unraveling the polygenic architecture of complex traits using blood eQTL metaanalysis (293 citations)
  • Genome-wide Analyses Identify KIF5A as a Novel ALS Gene (215 citations)
  • Prognosis for patients with amyotrophic lateral sclerosis: development and validation of a personalised prediction model (131 citations)

In his most recent research, the most cited papers focused on:

  • Gene
  • Internal medicine
  • Mutation

His scientific interests lie mostly in Amyotrophic lateral sclerosis, Genetics, Computational biology, Genome-wide association study and Genome. His research integrates issues of Biomarker, Survival analysis and Case-control study in his study of Amyotrophic lateral sclerosis. His work in Gene, Genetic association, Mutation, Allele and Phenotype is related to Genetics.

Jan H. Veldink has researched Genetic association in several fields, including Quantitative trait locus, Expression quantitative trait loci and Genomics. Genome-wide association study is a primary field of his research addressed under Single-nucleotide polymorphism. His work in the fields of Single-nucleotide polymorphism, such as Linkage disequilibrium, overlaps with other areas such as Human leukocyte antigen.

This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.

Best Publications

Genome-wide association study identifies five new schizophrenia loci

Stephan Ripke;Alan R. Sanders;Kenneth S. Kendler;Douglas F. Levinson.
Nature Genetics (2011)

2508 Citations

A reference panel of 64,976 haplotypes for genotype imputation

Shane McCarthy;Sayantan Das;Warren Kretzschmar;Olivier Delaneau.
Nature Genetics (2016)

2046 Citations

Systematic identification of trans eQTLs as putative drivers of known disease associations

Harm-Jan Westra;Marjolein J Peters;Tõnu Esko;Hanieh Yaghootkar.
Nature Genetics (2013)

1692 Citations

Multiple common variants for celiac disease influencing immune gene expression

Patrick C. A. Dubois;Gosia Trynka;Lude Franke;Lude Franke;Karen A. Hunt.
Nature Genetics (2010)

1069 Citations

Exome sequencing in amyotrophic lateral sclerosis identifies risk genes and pathways

Elizabeth T. Cirulli;Brittany N Lasseigne;Slave Petrovski;Peter C Sapp.
Science (2015)

831 Citations

Whole-genome sequence variation, population structure and demographic history of the Dutch population

Laurent C. Francioli;Androniki Menelaou;Sara L. Pulit;Freerk van Dijk.
Nature Genetics (2014)

603 Citations

Controversies and priorities in amyotrophic lateral sclerosis

Martin R Turner;Orla Hardiman;Michael Benatar;Benjamin R Brooks.
Lancet Neurology (2013)

562 Citations

Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis

Wouter van Rheenen;Aleksey Shatunov;Annelot M. Dekker;Russell L. McLaughlin.
Nature Genetics (2016)

456 Citations

Trans-eQTLs reveal that independent genetic variants associated with a complex phenotype converge on intermediate genes, with a major role for the HLA.

Rudolf S. N. Fehrmann;Ritsert C. Jansen;Jan H. Veldink;Harm-Jan Westra.
PLOS Genetics (2011)

411 Citations

Genome-wide Analyses Identify KIF5A as a Novel ALS Gene.

Aude Nicolas;Kevin P. Kenna;Alan E. Renton;Alan E. Renton;Nicola Ticozzi.
Neuron (2018)

399 Citations

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